Active Ingredient: PROCAINAMIDE HYDROCHLORIDE
Proprietary Name: PROCAINAMIDE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088533
Product Number: 001
Approval Date: Dec 3, 1984
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information